# FDA Inspection 853200 - Qiagen GmbH - September 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/qiagen-gmbh/b51741b2-bdd0-4473-b9bb-920265f3ea2c
Source feed: FDA_Inspections

> FDA Inspection 853200 for Qiagen GmbH on September 26, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 853200
- Company Name: Qiagen GmbH
- Inspection Date: 2013-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/qiagen-gmbh/ee8014e6-a226-4414-b52e-f5388c9834e3

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7